Showing 331 - 345 of 591 results
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Mahnke A, Plasek JM, Hoffman DG, Partridge NS, Foth WS, Waudby CJ,...McCarty CA [including McManus V.] (2014 January). A rural community's involvement in the design and usability testing of a computer-based informed consent process for the personalized medicine research project. American Journal of Medical Genetics Part A. 164(1):129-40.
PubMed ID: 24273095
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Shameer K, Denny J, Ding K, Jouni H, Crosslin D, De Andrade M,...Kullo IJ [including Peissig PL.] (2014 January). A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects. HUMAN GENETICS. 133(1):95-109.
PubMed ID: 24026423
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Kimmel SE, French B, Kasner SE, Johnson JA, Anderson JL, Gage BF,...Mazza, JJ [including Caldwell MD, Schmelzer, J.] (2013 December 12). A pharmacogenetic versus a clinical algorithm for warfarin dosing. N Engl J Med. 369(24):2283-93.
PubMed ID: 24251361
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Margolis KL, Davis BR, Baimbridge C, Ciocon JO, Cuyjet AB, Dart RA,...Williamson JD. (2013 December). Author response to lipid-lowering in African Americans in ALLHAT-optimism bias? J Clin Hypertens (Greenwich). 15(12):941.
PubMed ID: 24299695
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Liu J, Page D, Nassif H, Peissig PL, McCarty CA, Onitilo AA, Burnside E. Genetic variants improve breast cancer risk prediction on mammograms. AMIA Annu Symp Proc. 2013 November; 2013(eCollection 2013):876-85.
PubMed ID: 24551380
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McCarty CA, Berg RL, Rottscheit CM, Dart RA. (2013 November). The use of dietary supplements and their association with blood pressure in a large Midwestern cohort. BMC Complement Altern Med. 13 :339.
PubMed ID: 24283381
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Denny J, Bastarache L, Ritchie MD, Carroll R, Zink R, Mosley J,...Roden DM [including Peissig PL, Brilliant MH.] (2013 November). Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data. NATURE BIOTECHNOLOGY. 31(12):1102-1111.
PubMed ID: 24270849
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Gottesman O, Kuivaniemi H, Tromp G, Faucett W, Li R, Manolio T,...Peissig P [including Brilliant MH.] (2013 October). The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future. GENETICS IN MEDICINE. 15(10):761-71.
PubMed ID: 23743551
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McPherson EW, Cold CJ. (2013 October). Severe Pallister-Hall syndrome with persistent urogenital sinus, renal agenesis, imperforate anus, bilateral hypothalamic hamartomas, and severe skeletal anomalies. American Journal of Medical Genetics Part A. 161(10):2666-9.
PubMed ID: 23950073
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Chute CG, Ullman-Cullere M, Wood G, Lin S, He M, Pathak J. (2013 October). Some experiences and opportunities for big data in translational research. GENETICS IN MEDICINE. 15(10):802-809.
PubMed ID: 24008998
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Hartzler A, McCarty CA, Rasmussen LV, Williams M, Brilliant MH, Bowton E,...Trinidad S. (2013 October). Stakeholder engagement: a key component of integrating genomic information into electronic health records. GENETICS IN MEDICINE. 15(10):792-801.
PubMed ID: 24030437
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Kho A, Rasmussen LV, Connolly J, Peissig PL, Starren J, Hakonarson H, Hayes M. (2013 October). Practical challenges in integrating genomic data into the electronic health record. GENETICS IN MEDICINE. 15(10):772-8.
PubMed ID: 24071798
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Ji Y, Biernacka JM, Hebbring S, Chai Y, Jenkins GD, Batzler A,...Mrazek DA. (2013 October). Pharmacogenomics of selective serotonin reuptake inhibitor treatment for major depressive disorder: genome-wide associations and functional genomics. Pharmacogenomics J.. 13(5):456-63.
PubMed ID: 22907730
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Kimmel SE, French B, Anderson JL, Gage BF, Johnson JA, Rosenberg Y,...Ellenberg J [including Caldwell MD.] (2013 September). Rationale and design of the Clarification of Optimal Anticoagulation through Genetics trial. AMERICAN HEART JOURNAL. 166(3):435-41.
PubMed ID: 24016491
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Zhou Z, He M, Brilliant M, Brautbar A, Miller A, Weichelt B, Lin S. (2013 September). PS3-2: Informatics Challenges to Implement Pharmacogenetics to Clinical Practice. Clin Med Res. 11(3):147-148.
